Evidence map›Paper›PMID 22966001›Full record

ArticleThe Journal of experimental medicine2012

Neuropilin 1 is expressed on thymus-derived natural regulatory T cells, but not mucosa-generated induced Foxp3+ T reg cells.

Jonathan M Weiss, Angelina M Bilate, Michael Gobert, Yi Ding, Maria A Curotto de Lafaille, Christopher N Parkhurst, Huizhong Xiong, Jayashree Dolpady, Alan B Frey, Maria Grazia Ruocco and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 374 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
374citing papers in PubMed, 1 pooled it
25.4field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

374 citing papers in PubMed, 1 synthesis or guideline pooled it, 593 citations in OpenAlex.

  1. Pooled it
  2. Regulatory T cells in the skin: Origin, function, and plasticity.JID innovations : skin science from molecules to population health · 2026
    Review
  3. Review
  4. Regulatory T cells in cancer and inflammation.Signal transduction and targeted therapy · 2026
    Review
  5. Article
  6. Review
  7. HSPCs and TScience advances · 2026
    Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article

314 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors at 7 institutions in 4 countries.

Jonathan M WeissKimmel Center for Biology and Medicine at the Skirball Institute, New York University School of Medicine, New York, NY 10016, USA.
Angelina M Bilate
Michael Gobert
Yi Ding
Maria A Curotto de Lafaille
Christopher N Parkhurst
Huizhong Xiong
Jayashree Dolpady
Alan B Frey
Maria Grazia Ruocco
Yi Yang
Stefan Floess
Jochen Huehn
Soyoung Oh
Ming O Li
Rachel E Niec
Alexander Y Rudensky
Michael L Dustin
Dan R Littman
Juan J Lafaille
New York University · USInstitute of Biomedical Science · GBMemorial Sloan Kettering Cancer Center · USHelmholtz Centre for Infection Research · DEHoward Hughes Medical Institute · USNYU Langone Health · USSingapore Immunology Network · SG

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ADRIANA HEGUY · 1985 to 2026
$83.1M
Weill Cornell/Rockefeller/Sloan-Kettering MST ProgramT32GM007739 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI HSU, KATHARINE C · 1985 to 2023
$51.1M
Self Peptides Bound to MHC Class II In T Cell SelectionR37AI034206 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI RUDENSKY, ALEXANDER Y · 2009 to 2018
$4.8M
NCI NIH HHS 5 P30CA16087-31NCI NIH HHS P30 CA016087NIAID NIH HHS R37 AI034206NIGMS NIH HHS T32 GM007739
6 · The paper itself

Abstract

Foxp3 activity is essential for the normal function of the immune system. Two types of regulatory T (T reg) cells express Foxp3, thymus-generated natural T reg (nT reg) cells, and peripherally generated adaptive T reg (iT reg) cells. These cell types have complementary functions. Until now, it has not been possible to distinguish iT reg from nT reg cells in vivo based solely on surface markers. We report here that Neuropilin 1 (Nrp1) is expressed at high levels by most nT reg cells; in contrast, mucosa-generated iT reg and other noninflammatory iT reg cells express low levels of Nrp1. We found that Nrp1 expression is under the control of TGF-β. By tracing nT reg and iT reg cells, we could establish that some tumors have a very large proportion of infiltrating iT reg cells. iT reg cells obtained from highly inflammatory environments, such as the spinal cords of mice with spontaneous autoimmune encephalomyelitis (EAE) and the lungs of mice with chronic asthma, express Nrp1. In the same animals, iT reg cells in secondary lymphoid organs remain Nrp1(low). We also determined that, in spontaneous EAE, iT reg cells help to establish a chronic phase of the disease.

Indexed as

AnimalsCell LineageCell MembraneForkhead Transcription FactorsGene Expression RegulationInflammationIntestinal MucosaIntestinesLymphocyte ActivationLymphocytes, Tumor-InfiltratingMetagenomeMiceMice, TransgenicMucous MembraneNeuropilin-1Thymus GlandForkhead Transcription FactorsFoxp3 protein, mouseNeuropilin-1Transforming Growth Factor beta

Identifiers

PMID22966001
PMCPMC3457733
OpenAlexW2147638016

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.